JPH0572685A - 写真ハロゲン化銀材料及びプロセス - Google Patents

写真ハロゲン化銀材料及びプロセス

Info

Publication number: JPH0572685A
Authority: JP; Japan
Prior art keywords: coupler; component; group; photographic; inh
Prior art date: 1991-03-22
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.): Pending

Application number

JP6447192A

Other languages

English (en)

Japanese (ja)

Inventor

Paul A Burns

アンドリユーバーンズポール

Jerrold N Poslusny

ニールポスルスニージエロルド

Richard P Szajewski

ピータースザジエウスキリチヤード

Robert C Stewart

チヤールズスチユアートロバート

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Eastman Kodak Co

Original Assignee

Eastman Kodak Co

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1991-03-22

Filing date

1992-03-23

Publication date

1993-03-26

1992-03-23 Application filed by Eastman Kodak Co filed Critical Eastman Kodak Co

1993-03-26 Publication of JPH0572685A publication Critical patent/JPH0572685A/ja

Status Pending legal-status Critical Current

Links

-1 Silver halide Chemical class 0.000 title claims abstract description 42
229910052709 silver Inorganic materials 0.000 title claims abstract description 34
239000004332 silver Substances 0.000 title claims abstract description 34
239000000463 material Substances 0.000 title claims abstract description 21
238000000034 method Methods 0.000 title description 8
230000008569 process Effects 0.000 title description 4
239000003112 inhibitor Substances 0.000 claims abstract description 59
239000000839 emulsion Substances 0.000 claims abstract description 42
238000011161 development Methods 0.000 claims abstract description 35
238000012545 processing Methods 0.000 claims abstract description 17
125000004432 carbon atom Chemical group C* 0.000 claims abstract description 16
150000003568 thioethers Chemical class 0.000 claims abstract description 11
229910052799 carbon Inorganic materials 0.000 claims abstract description 10
JJJPTTANZGDADF-UHFFFAOYSA-N thiadiazole-4-thiol Chemical compound SC1=CSN=N1 JJJPTTANZGDADF-UHFFFAOYSA-N 0.000 claims abstract description 7
229920006395 saturated elastomer Polymers 0.000 claims abstract description 4
229910052717 sulfur Inorganic materials 0.000 claims description 12
125000004434 sulfur atom Chemical group 0.000 claims description 3
230000000694 effects Effects 0.000 abstract description 20
239000003999 initiator Substances 0.000 abstract 1
239000010410 layer Substances 0.000 description 51
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 48
239000000126 substance Substances 0.000 description 46
150000001875 compounds Chemical class 0.000 description 36
239000000975 dye Substances 0.000 description 25
238000006243 chemical reaction Methods 0.000 description 23
239000003795 chemical substances by application Substances 0.000 description 23
125000000217 alkyl group Chemical group 0.000 description 22
230000000269 nucleophilic effect Effects 0.000 description 21
238000011160 research Methods 0.000 description 20
239000000203 mixture Substances 0.000 description 19
125000003118 aryl group Chemical group 0.000 description 16
239000011229 interlayer Substances 0.000 description 14
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 12
IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 12
229910052739 hydrogen Inorganic materials 0.000 description 11
239000001257 hydrogen Substances 0.000 description 11
239000007787 solid Substances 0.000 description 11
WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 9
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
230000008878 coupling Effects 0.000 description 9
238000010168 coupling process Methods 0.000 description 9
238000005859 coupling reaction Methods 0.000 description 9
108010010803 Gelatin Proteins 0.000 description 7
125000003545 alkoxy group Chemical group 0.000 description 7
239000008273 gelatin Substances 0.000 description 7
229920000159 gelatin Polymers 0.000 description 7
235000019322 gelatine Nutrition 0.000 description 7
235000011852 gelatine desserts Nutrition 0.000 description 7
125000000623 heterocyclic group Chemical group 0.000 description 7
150000002431 hydrogen Chemical group 0.000 description 7
239000012299 nitrogen atmosphere Substances 0.000 description 7
239000000047 product Substances 0.000 description 7
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 6
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 6
230000002829 reductive effect Effects 0.000 description 6
239000011593 sulfur Substances 0.000 description 6
BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 5
125000004429 atom Chemical group 0.000 description 5
229910052736 halogen Inorganic materials 0.000 description 5
238000010534 nucleophilic substitution reaction Methods 0.000 description 5
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 5
230000027756 respiratory electron transport chain Effects 0.000 description 5
238000001228 spectrum Methods 0.000 description 5
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 4
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
230000015572 biosynthetic process Effects 0.000 description 4
150000001721 carbon Chemical group 0.000 description 4
230000000052 comparative effect Effects 0.000 description 4
239000013078 crystal Substances 0.000 description 4
125000004122 cyclic group Chemical group 0.000 description 4
230000002349 favourable effect Effects 0.000 description 4
150000002367 halogens Chemical class 0.000 description 4
125000005647 linker group Chemical group 0.000 description 4
BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 4
ZUNKMNLKJXRCDM-UHFFFAOYSA-N silver bromoiodide Chemical compound [Ag].IBr ZUNKMNLKJXRCDM-UHFFFAOYSA-N 0.000 description 4
238000006467 substitution reaction Methods 0.000 description 4
241001479434 Agfa Species 0.000 description 3
CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 3
BUGBHKTXTAQXES-UHFFFAOYSA-N Selenium Chemical compound [Se] BUGBHKTXTAQXES-UHFFFAOYSA-N 0.000 description 3
125000004414 alkyl thio group Chemical group 0.000 description 3
125000004104 aryloxy group Chemical group 0.000 description 3
238000003776 cleavage reaction Methods 0.000 description 3
238000012937 correction Methods 0.000 description 3
238000009792 diffusion process Methods 0.000 description 3
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 3
238000001914 filtration Methods 0.000 description 3
238000002844 melting Methods 0.000 description 3
230000008018 melting Effects 0.000 description 3
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
238000012544 monitoring process Methods 0.000 description 3
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 3
NLKNQRATVPKPDG-UHFFFAOYSA-M potassium iodide Chemical compound [K+].[I-] NLKNQRATVPKPDG-UHFFFAOYSA-M 0.000 description 3
230000007017 scission Effects 0.000 description 3
229910052711 selenium Inorganic materials 0.000 description 3
239000011669 selenium Substances 0.000 description 3
230000003381 solubilizing effect Effects 0.000 description 3
239000003381 stabilizer Substances 0.000 description 3
125000001424 substituent group Chemical group 0.000 description 3
238000003786 synthesis reaction Methods 0.000 description 3
229910052714 tellurium Inorganic materials 0.000 description 3
PORWMNRCUJJQNO-UHFFFAOYSA-N tellurium atom Chemical compound [Te] PORWMNRCUJJQNO-UHFFFAOYSA-N 0.000 description 3
125000000101 thioether group Chemical group 0.000 description 3
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
MBIZXFATKUQOOA-UHFFFAOYSA-N 1,3,4-thiadiazole Chemical compound C1=NN=CS1 MBIZXFATKUQOOA-UHFFFAOYSA-N 0.000 description 2
BIGYLAKFCGVRAN-UHFFFAOYSA-N 1,3,4-thiadiazolidine-2,5-dithione Chemical compound S=C1NNC(=S)S1 BIGYLAKFCGVRAN-UHFFFAOYSA-N 0.000 description 2
CEZVGLHZVYEJBR-UHFFFAOYSA-N 2,5-didodecylbenzene-1,4-diol Chemical compound CCCCCCCCCCCCC1=CC(O)=C(CCCCCCCCCCCC)C=C1O CEZVGLHZVYEJBR-UHFFFAOYSA-N 0.000 description 2
JLAMDELLBBZOOX-UHFFFAOYSA-N 3h-1,3,4-thiadiazole-2-thione Chemical compound SC1=NN=CS1 JLAMDELLBBZOOX-UHFFFAOYSA-N 0.000 description 2
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
YLQBMQCUIZJEEH-UHFFFAOYSA-N Furan Chemical compound C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 2
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 description 2
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical class [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 description 2
YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical compound C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 description 2
125000002015 acyclic group Chemical group 0.000 description 2
125000004453 alkoxycarbonyl group Chemical group 0.000 description 2
125000002947 alkylene group Chemical group 0.000 description 2
125000001769 aryl amino group Chemical group 0.000 description 2
125000005110 aryl thio group Chemical group 0.000 description 2
125000002837 carbocyclic group Chemical group 0.000 description 2
125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 2
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 2
239000007795 chemical reaction product Substances 0.000 description 2
125000001309 chloro group Chemical group Cl* 0.000 description 2
230000002950 deficient Effects 0.000 description 2
230000009034 developmental inhibition Effects 0.000 description 2
DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 2
238000000921 elemental analysis Methods 0.000 description 2
125000001153 fluoro group Chemical group F* 0.000 description 2
239000012634 fragment Substances 0.000 description 2
239000011521 glass Substances 0.000 description 2
125000005843 halogen group Chemical group 0.000 description 2
125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
239000005457 ice water Substances 0.000 description 2
230000002401 inhibitory effect Effects 0.000 description 2
AJDUTMFFZHIJEM-UHFFFAOYSA-N n-(9,10-dioxoanthracen-1-yl)-4-[4-[[4-[4-[(9,10-dioxoanthracen-1-yl)carbamoyl]phenyl]phenyl]diazenyl]phenyl]benzamide Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C=CC=C2NC(=O)C(C=C1)=CC=C1C(C=C1)=CC=C1N=NC(C=C1)=CC=C1C(C=C1)=CC=C1C(=O)NC1=CC=CC2=C1C(=O)C1=CC=CC=C1C2=O AJDUTMFFZHIJEM-UHFFFAOYSA-N 0.000 description 2
125000001624 naphthyl group Chemical group 0.000 description 2
229910000510 noble metal Inorganic materials 0.000 description 2
125000000962 organic group Chemical group 0.000 description 2
229910052760 oxygen Inorganic materials 0.000 description 2
229910000027 potassium carbonate Inorganic materials 0.000 description 2
239000002243 precursor Substances 0.000 description 2
238000002360 preparation method Methods 0.000 description 2
230000005855 radiation Effects 0.000 description 2
230000009467 reduction Effects 0.000 description 2
230000001235 sensitizing effect Effects 0.000 description 2
239000000741 silica gel Substances 0.000 description 2
229910002027 silica gel Inorganic materials 0.000 description 2
125000000547 substituted alkyl group Chemical group 0.000 description 2
229940124530 sulfonamide Drugs 0.000 description 2
150000003456 sulfonamides Chemical class 0.000 description 2
239000001043 yellow dye Substances 0.000 description 2
GVEYRUKUJCHJSR-UHFFFAOYSA-N (4-azaniumyl-3-methylphenyl)-ethyl-(2-hydroxyethyl)azanium;sulfate Chemical compound OS(O)(=O)=O.OCCN(CC)C1=CC=C(N)C(C)=C1 GVEYRUKUJCHJSR-UHFFFAOYSA-N 0.000 description 1
150000005207 1,3-dihydroxybenzenes Chemical class 0.000 description 1
CBCKQZAAMUWICA-UHFFFAOYSA-N 1,4-phenylenediamine Chemical group NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 description 1
GGZHVNZHFYCSEV-UHFFFAOYSA-N 1-Phenyl-5-mercaptotetrazole Chemical compound SC1=NN=NN1C1=CC=CC=C1 GGZHVNZHFYCSEV-UHFFFAOYSA-N 0.000 description 1
JKFYKCYQEWQPTM-UHFFFAOYSA-N 2-azaniumyl-2-(4-fluorophenyl)acetate Chemical compound OC(=O)C(N)C1=CC=C(F)C=C1 JKFYKCYQEWQPTM-UHFFFAOYSA-N 0.000 description 1
125000004200 2-methoxyethyl group Chemical group [H]C([H])([H])OC([H])([H])C([H])([H])* 0.000 description 1
CMLFRMDBDNHMRA-UHFFFAOYSA-N 2h-1,2-benzoxazine Chemical compound C1=CC=C2C=CNOC2=C1 CMLFRMDBDNHMRA-UHFFFAOYSA-N 0.000 description 1
CWLKGDAVCFYWJK-UHFFFAOYSA-N 3-aminophenol Chemical class NC1=CC=CC(O)=C1 CWLKGDAVCFYWJK-UHFFFAOYSA-N 0.000 description 1
XRZDIHADHZSFBB-UHFFFAOYSA-N 3-oxo-n,3-diphenylpropanamide Chemical class C=1C=CC=CC=1NC(=O)CC(=O)C1=CC=CC=C1 XRZDIHADHZSFBB-UHFFFAOYSA-N 0.000 description 1
RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
CWNSVVHTTQBGQB-UHFFFAOYSA-N N,N-Diethyldodecanamide Chemical compound CCCCCCCCCCCC(=O)N(CC)CC CWNSVVHTTQBGQB-UHFFFAOYSA-N 0.000 description 1
241000700159 Rattus Species 0.000 description 1
229910021607 Silver chloride Inorganic materials 0.000 description 1
229910021612 Silver iodide Inorganic materials 0.000 description 1
MPLZNPZPPXERDA-UHFFFAOYSA-N [4-(diethylamino)-2-methylphenyl]azanium;chloride Chemical compound [Cl-].CC[NH+](CC)C1=CC=C(N)C(C)=C1 MPLZNPZPPXERDA-UHFFFAOYSA-N 0.000 description 1
SJOOOZPMQAWAOP-UHFFFAOYSA-N [Ag].BrCl Chemical compound [Ag].BrCl SJOOOZPMQAWAOP-UHFFFAOYSA-N 0.000 description 1
HOLVRJRSWZOAJU-UHFFFAOYSA-N [Ag].ICl Chemical compound [Ag].ICl HOLVRJRSWZOAJU-UHFFFAOYSA-N 0.000 description 1
239000006096 absorbing agent Substances 0.000 description 1
230000009471 action Effects 0.000 description 1
125000002252 acyl group Chemical group 0.000 description 1
230000002411 adverse Effects 0.000 description 1
125000003342 alkenyl group Chemical group 0.000 description 1
125000003282 alkyl amino group Chemical group 0.000 description 1
125000004390 alkyl sulfonyl group Chemical group 0.000 description 1
125000004422 alkyl sulphonamide group Chemical group 0.000 description 1
IYABWNGZIDDRAK-UHFFFAOYSA-N allene Chemical group C=C=C IYABWNGZIDDRAK-UHFFFAOYSA-N 0.000 description 1
125000003368 amide group Chemical group 0.000 description 1
229940051880 analgesics and antipyretics pyrazolones Drugs 0.000 description 1
239000002216 antistatic agent Substances 0.000 description 1
125000005161 aryl oxy carbonyl group Chemical group 0.000 description 1
125000000732 arylene group Chemical group 0.000 description 1
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
229910052797 bismuth Inorganic materials 0.000 description 1
JCXGWMGPZLAOME-UHFFFAOYSA-N bismuth atom Chemical compound [Bi] JCXGWMGPZLAOME-UHFFFAOYSA-N 0.000 description 1
238000004061 bleaching Methods 0.000 description 1
239000007844 bleaching agent Substances 0.000 description 1
125000001246 bromo group Chemical group Br* 0.000 description 1
125000004106 butoxy group Chemical group [*]OC([H])([H])C([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 1
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
229910052793 cadmium Inorganic materials 0.000 description 1
BDOSMKKIYDKNTQ-UHFFFAOYSA-N cadmium atom Chemical compound [Cd] BDOSMKKIYDKNTQ-UHFFFAOYSA-N 0.000 description 1
125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 description 1
125000005521 carbonamide group Chemical group 0.000 description 1
125000004181 carboxyalkyl group Chemical group 0.000 description 1
229910052798 chalcogen Inorganic materials 0.000 description 1
150000001787 chalcogens Chemical class 0.000 description 1
238000012512 characterization method Methods 0.000 description 1
125000000068 chlorophenyl group Chemical group 0.000 description 1
239000011248 coating agent Substances 0.000 description 1
238000000576 coating method Methods 0.000 description 1
239000013068 control sample Substances 0.000 description 1
238000013270 controlled release Methods 0.000 description 1
229910052802 copper Inorganic materials 0.000 description 1
239000010949 copper Substances 0.000 description 1
125000004093 cyano group Chemical group *C#N 0.000 description 1
125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
239000000539 dimer Substances 0.000 description 1
238000006073 displacement reaction Methods 0.000 description 1
238000009826 distribution Methods 0.000 description 1
238000001035 drying Methods 0.000 description 1
125000006575 electron-withdrawing group Chemical group 0.000 description 1
238000010828 elution Methods 0.000 description 1
229960003750 ethyl chloride Drugs 0.000 description 1
238000011156 evaluation Methods 0.000 description 1
230000001747 exhibiting effect Effects 0.000 description 1
239000010946 fine silver Substances 0.000 description 1
PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
229910052737 gold Inorganic materials 0.000 description 1
239000010931 gold Substances 0.000 description 1
150000004820 halides Chemical class 0.000 description 1
125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 1
230000007062 hydrolysis Effects 0.000 description 1
238000006460 hydrolysis reaction Methods 0.000 description 1
125000004464 hydroxyphenyl group Chemical group 0.000 description 1
PTFYQSWHBLOXRZ-UHFFFAOYSA-N imidazo[4,5-e]indazole Chemical class C1=CC2=NC=NC2=C2C=NN=C21 PTFYQSWHBLOXRZ-UHFFFAOYSA-N 0.000 description 1
230000006872 improvement Effects 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
125000002346 iodo group Chemical group I* 0.000 description 1
238000002386 leaching Methods 0.000 description 1
239000007788 liquid Substances 0.000 description 1
239000000314 lubricant Substances 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
230000000873 masking effect Effects 0.000 description 1
239000006224 matting agent Substances 0.000 description 1
230000007246 mechanism Effects 0.000 description 1
SNVLJLYUUXKWOJ-UHFFFAOYSA-N methylidenecarbene Chemical group C=[C] SNVLJLYUUXKWOJ-UHFFFAOYSA-N 0.000 description 1
210000004088 microvessel Anatomy 0.000 description 1
238000002156 mixing Methods 0.000 description 1
239000003607 modifier Substances 0.000 description 1
239000000178 monomer Substances 0.000 description 1
JJKACVAOVDKGLK-UHFFFAOYSA-N n-[3-(diethylamino)-2-ethylphenyl]methanesulfonamide;hydrochloride Chemical compound Cl.CCN(CC)C1=CC=CC(NS(C)(=O)=O)=C1CC JJKACVAOVDKGLK-UHFFFAOYSA-N 0.000 description 1
150000004780 naphthols Chemical class 0.000 description 1
125000004957 naphthylene group Chemical group 0.000 description 1
125000004433 nitrogen atom Chemical group N* 0.000 description 1
239000002667 nucleating agent Substances 0.000 description 1
238000007344 nucleophilic reaction Methods 0.000 description 1
230000003287 optical effect Effects 0.000 description 1
230000003647 oxidation Effects 0.000 description 1
238000007254 oxidation reaction Methods 0.000 description 1
239000001301 oxygen Substances 0.000 description 1
JOXIMZWYDAKGHI-UHFFFAOYSA-N p-toluenesulfonic acid Substances CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 1
125000002958 pentadecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
150000002989 phenols Chemical class 0.000 description 1
125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 description 1
125000005499 phosphonyl group Chemical group 0.000 description 1
239000004014 plasticizer Substances 0.000 description 1
239000004848 polyfunctional curative Substances 0.000 description 1
229920000642 polymer Polymers 0.000 description 1
239000002244 precipitate Substances 0.000 description 1
238000001556 precipitation Methods 0.000 description 1
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
230000001681 protective effect Effects 0.000 description 1
JEXVQSWXXUJEMA-UHFFFAOYSA-N pyrazol-3-one Chemical class O=C1C=CN=N1 JEXVQSWXXUJEMA-UHFFFAOYSA-N 0.000 description 1
MCSKRVKAXABJLX-UHFFFAOYSA-N pyrazolo[3,4-d]triazole Chemical class N1=NN=C2N=NC=C21 MCSKRVKAXABJLX-UHFFFAOYSA-N 0.000 description 1
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
238000006798 ring closing metathesis reaction Methods 0.000 description 1
125000006413 ring segment Chemical group 0.000 description 1
238000000926 separation method Methods 0.000 description 1
239000000377 silicon dioxide Substances 0.000 description 1
ADZWSOLPGZMUMY-UHFFFAOYSA-M silver bromide Chemical compound [Ag]Br ADZWSOLPGZMUMY-UHFFFAOYSA-M 0.000 description 1
229940045105 silver iodide Drugs 0.000 description 1
HKZLPVFGJNLROG-UHFFFAOYSA-M silver monochloride Chemical compound [Cl-].[Ag+] HKZLPVFGJNLROG-UHFFFAOYSA-M 0.000 description 1
230000003595 spectral effect Effects 0.000 description 1
125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
238000003756 stirring Methods 0.000 description 1
125000005504 styryl group Chemical group 0.000 description 1
125000003107 substituted aryl group Chemical group 0.000 description 1
125000004964 sulfoalkyl group Chemical group 0.000 description 1
125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 description 1
230000002194 synthesizing effect Effects 0.000 description 1
238000012360 testing method Methods 0.000 description 1
229910052716 thallium Inorganic materials 0.000 description 1
BKVIYDNLLOSFOA-UHFFFAOYSA-N thallium Chemical compound [Tl] BKVIYDNLLOSFOA-UHFFFAOYSA-N 0.000 description 1
VLLMWSRANPNYQX-UHFFFAOYSA-N thiadiazole Chemical compound C1=CSN=N1.C1=CSN=N1 VLLMWSRANPNYQX-UHFFFAOYSA-N 0.000 description 1
125000002813 thiocarbonyl group Chemical group *C(*)=S 0.000 description 1
229930192474 thiophene Natural products 0.000 description 1
125000003944 tolyl group Chemical group 0.000 description 1
230000001052 transient effect Effects 0.000 description 1
238000005406 washing Methods 0.000 description 1

Classifications

- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
- G03C7/00—Multicolour photographic processes or agents therefor; Regeneration of such processing agents; Photosensitive materials for multicolour processes
- G03C7/30—Colour processes using colour-coupling substances; Materials therefor; Preparing or processing such materials
- G03C7/305—Substances liberating photographically active agents, e.g. development-inhibiting releasing couplers
- G03C7/30541—Substances liberating photographically active agents, e.g. development-inhibiting releasing couplers characterised by the released group

Landscapes

Physics & Mathematics (AREA)
General Physics & Mathematics (AREA)
Silver Salt Photography Or Processing Solution Therefor (AREA)

JP6447192A 1991-03-22 1992-03-23 写真ハロゲン化銀材料及びプロセス Pending JPH0572685A (ja)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
US673885		1984-11-21
US67388591A	1991-03-22	1991-03-22

Publications (1)

Publication Number	Publication Date
JPH0572685A true JPH0572685A (ja)	1993-03-26

Family

ID=24704488

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP6447192A Pending JPH0572685A (ja)	1991-03-22	1992-03-23	写真ハロゲン化銀材料及びプロセス

Country Status (2)

Country	Link
EP (1)	EP0505008A3 (fr)
JP (1)	JPH0572685A (fr)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE102005004472A1 (de) *	2005-01-31	2006-08-10	Rhein Chemie Rheinau Gmbh	Verfahren zur Herstellung von Bis-DMTD

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US5006448A (en) *	1989-06-15	1991-04-09	Eastman Kodak Company	Photographic material and process
US5135839A (en) *	1990-11-13	1992-08-04	Eastman Kodak Company	Silver halide material with dir and bleach accelerator releasing couplers

1992
- 1992-03-19 EP EP19920200783 patent/EP0505008A3/en not_active Withdrawn
- 1992-03-23 JP JP6447192A patent/JPH0572685A/ja active Pending

Also Published As

Publication number	Publication date
EP0505008A2 (fr)	1992-09-23
EP0505008A3 (en)	1992-11-19

Publication	Publication Date	Title
JP2810764B2 (ja)	1998-10-15	写真ハロゲン化銀組成物
JP2561671B2 (ja)	1996-12-11	写真要素
US4628024A (en)	1986-12-09	Silver halide color photographic light-sensitive material
EP0403019B1 (fr)	1995-09-13	Matériau photographique et procédé
JP3195426B2 (ja)	2001-08-06	Ｄｉｒカプラー含有写真要素
EP0356925B1 (fr)	1995-05-24	Elément et procédé photographique comprenant un coupleur libérant un inhibiteur de développement et un coupleur formateur de colorant jaune
JPH0247650A (ja)	1990-02-16	カラー写真感光材料
EP0485965B1 (fr)	1998-10-14	Matériau photographique à l'halogénure d'argent et procédé
JPH07181644A (ja)	1995-07-21	反転カラー写真要素及びその処理方法
US5567577A (en)	1996-10-22	Photographic elements containing release compounds
US5612173A (en)	1997-03-18	One equivalent couplers and low PKA release dyes
US5021555A (en)	1991-06-04	Color photographic material
JPH0511414A (ja)	1993-01-22	ハロゲン化銀カラー写真感光材料
JP2001183782A (ja)	2001-07-06	多色写真要素
JP3247500B2 (ja)	2002-01-15	写真要素
JPH0572685A (ja)	1993-03-26	写真ハロゲン化銀材料及びプロセス
JP3281398B2 (ja)	2002-05-13	離脱性フィルター色素含有写真要素
JP2001209156A (ja)	2001-08-03	写真要素
JPH05249635A (ja)	1993-09-28	ハロゲン化銀写真要素における発色方法及び感光性要素
JPH05249603A (ja)	1993-09-28	過酸化物含有処理液で使用するためのブロックされた写真的に有用な化合物類を含んでなる写真要素
JPH06214358A (ja)	1994-08-05	イエロー色素形成性カプラー及びこれらを含むカラー写真要素
EP0443159B1 (fr)	1996-06-12	Coupleurs formateurs de cyan et produits photographiques de reproduction les contenant
JP2776587B2 (ja)	1998-07-16	写真要素
JPH0553264A (ja)	1993-03-05	ハロゲン化銀カラー写真感光材料
JPH04275546A (ja)	1992-10-01	現像促進剤放出化合物を含有する写真要素